Scleroderma Foundation Southern California Chapter

Organization Overview

Scleroderma Foundation Southern California Chapter is located in Los Angeles, CA. The organization was established in 1994. As of 12/2023, Scleroderma Foundation Southern California Chapter employed 2 individuals. This organization is an independent organization and not affiliated with a larger national or regional group of organizations. Scleroderma Foundation Southern California Chapter is a 501(c)(3) and as such, is described as a "Charitable or Religous organization or a private foundation" by the IRS.

For the year ending 12/2023, Scleroderma Foundation Southern California Chapter generated $274.8k in total revenue. This represents a relatively dramatic decline in revenue. Over the past 9 years, the organization has seen revenues fall by an average of (4.7%) each year. All expenses for the organization totaled $336.9k during the year ending 12/2023. You can explore the organizations financials more deeply in the financial statements section below.

Mission & Program ActivityExcerpts From the 990 Filing

TAX YEAR

2023

Describe the Organization's Mission:

Part 3 - Line 1

TO EMPOWER THE SCLERODERMA COMMUNITY TO LIVE BETTER LIVES.

Describe the Organization's Program Activity:

Part 3 - Line 4a

SUPPORT: PROVIDE PATIENT SUPPORT AND EDUCATION TO OVER 1000 PATIENTS AFFECTED BY SCLERODERMA IN CALIFORNIA WE WORK TO BUILD OVERALL AWARENESS OF THE DISEASE. THE FOUNDATION NOW HAS 26 COMMUNITY SUPPORT GROUPS. MOST GROUPS MEET BI-MONTHLY AND HAVE AN AVERAGE ATTENDANCE OF 25-20 PEOPLE. IN 2023 MANY OF OUR SUPPORT GROUPS TRANSITIONED BACK TO IN-PERSON MEETINGS AND WE WERE ABLE TO GROW TO REACH APPROXIMATELY 2000+ PATIENTS/CAREGIVERS AND FAMILY MEMBERS. WE WILL CONTINUE TO PROVIDE ONLINE MEETINGS AS WELL AS IN-PERSON MEETINGS. SUPPORT GROUPS PROVIDE A FORUM TO SHARE FEELINGS, CONCERNS, INFORMATION, AS WELL AS A PLACE TO OFFER PEER SUPPORT AND ENCOURAGEMENT. SOLICITATIONS OR RESEARCH PROJECTS ARE NOT CONDUCTED AT SUPPORT GROUP MEETINGS. SUPPORT GROUPS OFTEN FEATURE SPEAKERS SPECIALIZING IN SCLERODERMA OR RELATED TOPICS. ALL SUPPORT GROUPS ARE FREE OF CHARGE AND OPEN TO EVERYONE, INCLUDING PATIENTS, CAREGIVERS, FAMILY AND FRIENDS.


EDUCATION:IN 2023 THE SCLERODERMA FOUNDATION HOSTED AN ONLINE EDUCATION EVENT FOR PATIENTS, FAMILY MEMBERS AND CAREGIVERS WITH THE TOTAL NUMBER WHO BENEFITTED APPROXIMATELY 500.FOR MEDICAL PROFESSIONALS TO HELP THEM UNDERSTAND AND PROPERLY DIAGNOSIS SCLERODERMA EARLY, AND FOR PATIENTS TO HELP THEM AND COPE AND THRIVE WHILE LIVING WITH SCLERODERMA.


RESEARCH:WE CONTINUE TO SEEK RESEARCH PROJECTS TO FUND TO FIND A CURE TO END SCLERODERMA.


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Board, Officers & Key Employees

Name (title)Compensation
Dr Dan Furst
Acting President
$0
David Parker
Secretary
$0
Laura Fuhrman
Vice President
$0
Maria Salinas
Treasurer
$0
Peggy Hickman
Past President
$0
Chris Pettit
Vice President
$0

Financial Statements

Statement of Revenue
Federated campaigns$0
Membership dues$0
Fundraising events$264,280
Related organizations$0
Government grants $0
All other contributions, gifts, grants, and similar amounts not included above$76,208
Noncash contributions included in lines 1a–1f $0
Total Revenue from Contributions, Gifts, Grants & Similar$340,488
Total Program Service Revenue$0
Investment income $0
Tax Exempt Bond Proceeds $0
Royalties $0
Net Rental Income $0
Net Gain/Loss on Asset Sales $0
Net Income from Fundraising Events -$65,712
Net Income from Gaming Activities $0
Net Income from Sales of Inventory $0
Miscellaneous Revenue$0
Total Revenue $274,776

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